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67370-87-0

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67370-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67370-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67370-87:
(7*6)+(6*7)+(5*3)+(4*7)+(3*0)+(2*8)+(1*7)=150
150 % 10 = 0
So 67370-87-0 is a valid CAS Registry Number.

67370-87-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-1,5-diazacycloheptadecan-6-one

1.2 Other means of identification

Product number -
Other names 5-methyl-1,5-diaza-cycloheptadecan-6-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67370-87-0 SDS

67370-87-0Downstream Products

67370-87-0Relevant articles and documents

Transamidation Reactions. Part 11) N-Substituted 3-Aminopropanenitriles and 2-Aminoacetonitriles as Schiff-Base Equivalents

Askitoglu, Elefteria,Guggisberg, Armin,Hesse, Manfred

, p. 750 - 759 (2007/10/02)

In presence of a strong base, the 13-membered cyclic compound 3 yielded, by loss of acetonitrile or its equivalent, the bicyclic product 5 instead of the 17-membered compound 4 as expected (Scheme 2).Investigation of model compounds (Scheme 4) and of model reactions (Schemes 5 and 6) led to the conclusion that the reaction proceeds via an intermediate formaldehyde imine; a Schiff base, e. g. 3b (Scheme 5), which reacts intra- and intermolecularly with a nucleophile to form a Mannich-type product.It seems to be a general principle that N-substituted 3-aminopropanenitrile and 2-aminoacetonitrile derivatives behave in the presence of a strong base as Schiff-base equivalents (Scheme 5 and 6).

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